CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT
K-Number: K023463 · 2003-02-19
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Device Summary
Frequently Asked Questions
What is the CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT?
CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT is a medical device that received FDA 510(k) clearance on 2003-02-19. The listed applicant is Cryo Vascular Systems, Inc.. The 510(k) number is K023463.
When did CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT receive FDA 510(k) clearance?
CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT received FDA 510(k) clearance on 2003-02-19, under 510(k) number K023463.
Who is the listed applicant for CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT?
The FDA 510(k) record lists Cryo Vascular Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT?
The FDA product code for CVSI PERIPHERAL BALLOON CATHETER; CVSI CATHETER INFLATION UNIT is DQY.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Cryo Vascular Systems, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DQY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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